Tag | Content |
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EnhancerAtlas ID | HS030-00772 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:40252490-40253820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:40253426-40253441 | TGAACTTTGTCCCTC | - | 6.15 | Hnf4a | MA0114.3 | chr1:40253424-40253440 | GCTGAACTTTGTCCCT | - | 6.05 | RARA | MA0729.1 | chr1:40253656-40253674 | CCATGACCCTTAGACCTT | - | 6.29 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATGGCTGCC TCCTGCTGCT CGCCTCCACC ACCAGCTCTG GGTTGCGGGA AGCAGAGGCT 60 TGGCCATGCC CTCTTCTGTC CTAGTGTAGG AAGCAAATGG CTGATGGCCC CACAAAACCT 120 GCTGCGGCTC AGTCCCCTGT TTTCCTCAGC CCAGACTCCT CAGAAAGGTC TCTGCACCTT 180 GAAAGCCTGA CCTGACAACA GAAATGTCAT CTCTTTGAGC CCTGGATGGA CAGTCAGGCT 240 TCCTGGGCCT GTCCTGGCTC AGCAGCGTAG AGGCTGCGCT GTCCTAGGCA TGGCGCTGCC 300 TCTCTGAGCC TCACTGTCCT CATCTGGGAG ATGGGGATGA AGACCGTGGC TGTTATCAGG 360 GTTGTCGGGA GGATGAAGAA TTAATGATGC TGTCTGTGGA GGGAGGCTGA TGGCCGGGGC 420 CAGGGACCCT CTCCCTCCTC TCAGCCCCAC AGCTCCCCGA CTTTGGGCTG ATCTGTGGTC 480 CTTGGTTCCC CAGACCCCAG ACTGTCACTA GCCACAGACA GGAGGCAAAG CAGATGGGTG 540 ACCTGACCAA TAGTAACTAC ATGACCATAG ACCAAAGAGT TTAGTACTGG AAAAAAAATC 600 TCTGAGATCT TAGGGAATAA ATAGCTCCAG GGTTTGATAC AAGATATTTG CAGACAGGAA 660 AAGCCGGGCT TTGCCTGGGA GAACAAAGTG GGTCCAGCTG CCCACTGGAC CATTCCACAG 720 GACTGGACAC TCACCCCATA CCAGATCACA TCCCAGGTGT TGGGCCCAGG GTGACAAGGC 780 AACAGTCCCT GCCCCAGCGA GCTGAGTTTG CTCCTTCCCC AGCCGCCCCC CTGACAGCCG 840 CACCCCACCC AGGCTCCGCA CAGAGAAGAG CCTGCTGTGG ACTCAGGGCA CGCGACTCAG 900 CTCTGGTCAC TCCGATGTGA CCACAGGTTT CCACGCTGAA CTTTGTCCCT CTCCTCAGTA 960 CTGCCCTTAT CACAGTGACA GCATCCCGGC CTCTGTTTAC TCACCTGTCT CCCCAGGACC 1020 AGGCTGTCTT CCCGGGGCAG CCCAGGTGGG CAAAGACATC ACCTGATTCT TACTCCTGGG 1080 TGTGTTTGGG GCAGGGTGAA GGCAGCGCCT GGGAGTCCAC AGTCCCCCAC ACTCTGCTCC 1140 TGACCACCCC GCAGCCCAGG GGGCCCCCAT GACCCTTAGA CCTTCCCTAA CCACGGCGGT 1200 CCCACTCCCC TGTGGTTCGC GTCCACCGTC TGTGACTCCC CGTTCGGCCA GGGCCCGGCA 1260 CAGCCCGCGG ATGCGCGCCC CTCCCCTGCA GCCAGCTTAC TCCGAGGGTC CCCGCGCGGG 1320 CGGCCGCACT 1330
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